Variant report

Variant	rs17010176
Chromosome Location	chr2:30978370-30978371
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:6)

rs_ID	r²[population]
rs17010130	1.00[JPT][hapmap];0.96[YRI][hapmap];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17010175	1.00[JPT][hapmap];0.85[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6721423	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs6739240	1.00[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs7567387	0.87[ASN][1000 genomes]
rs7580779	0.85[AMR][1000 genomes];0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533886	chr2:30130019-31068764	ZNF genes & repeats Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv873770	chr2:30952987-30984850	Weak transcription Enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
3	nsv520269	chr2:30958137-30988375	Weak transcription Bivalent Enhancer Strong transcription Enhancers Genic enhancers ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv456019	chr2:30968228-30984850	Weak transcription Bivalent Enhancer Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a
5	nsv581267	chr2:30968228-30984850	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:30960400-30980000	Weak transcription	Brain Hippocampus Middle	brain
2	chr2:30961600-30978400	Weak transcription	Pancreas	Pancrea
3	chr2:30964400-30978600	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr2:30965800-30999400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr2:30967400-30978800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr2:30968200-30985600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr2:30970600-30978800	Weak transcription	Duodenum Mucosa	Duodenum
8	chr2:30971000-30984800	Weak transcription	Stomach Mucosa	stomach
9	chr2:30974400-30978800	Weak transcription	Rectal Mucosa Donor 31	rectum
10	chr2:30976400-30978800	Weak transcription	Fetal Intestine Small	intestine
11	chr2:30977800-30978400	Weak transcription	Rectal Mucosa Donor 29	rectum
12	chr2:30977800-30979200	Weak transcription	Gastric	stomach
13	chr2:30978000-30980800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr2:30978200-30979000	Enhancers	Spleen	Spleen
15	chr2:30978200-30980000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:30978200-30980200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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